Published in Alzheimer Dis Assoc Disord on March 31, 2017
Genetic variation and population structure in native Americans. PLoS Genet (2007) 4.87
A genomewide admixture map for Latino populations. Am J Hum Genet (2007) 4.71
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nat Genet (2006) 3.54
Reconstructing Native American population history. Nature (2012) 3.49
Brain imaging and fluid biomarker analysis in young adults at genetic risk for autosomal dominant Alzheimer's disease in the presenilin 1 E280A kindred: a case-control study. Lancet Neurol (2012) 3.48
A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron (2010) 3.31
Geographic patterns of genome admixture in Latin American Mestizos. PLoS Genet (2008) 3.07
Alzheimer's Prevention Initiative: a plan to accelerate the evaluation of presymptomatic treatments. J Alzheimers Dis (2011) 2.78
Apolipoprotein Eepsilon4 modifies Alzheimer's disease onset in an E280A PS1 kindred. Ann Neurol (2003) 2.72
Florbetapir PET analysis of amyloid-β deposition in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional study. Lancet Neurol (2012) 2.65
Pre-dementia clinical stages in presenilin 1 E280A familial early-onset Alzheimer's disease: a retrospective cohort study. Lancet Neurol (2011) 2.65
Y-chromosome evidence for differing ancient demographic histories in the Americas. Am J Hum Genet (2003) 1.84
Ancestry-related assortative mating in Latino populations. Genome Biol (2009) 1.79
Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica. Hum Genet (2003) 1.76
Development of a panel of genome-wide ancestry informative markers to study admixture throughout the Americas. PLoS Genet (2012) 1.74
Covert matching of unfamiliar faces in a case of prosopagnosia: an ERP study. Cortex (2003) 1.58
Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease. Neurobiol Aging (2013) 1.53
Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11. Am J Hum Genet (2004) 1.49
Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet (2008) 1.48
Hippocampal hyperactivation in presymptomatic familial Alzheimer's disease. Ann Neurol (2010) 1.45
Visual short-term memory binding deficits in familial Alzheimer's disease. Brain (2010) 1.32
Genetic make up and structure of Colombian populations by means of uniparental and biparental DNA markers. Am J Phys Anthropol (2010) 1.29
The Alzheimer's prevention initiative composite cognitive test score: sample size estimates for the evaluation of preclinical Alzheimer's disease treatments in presenilin 1 E280A mutation carriers. J Clin Psychiatry (2014) 1.25
African ancestry is associated with risk of asthma and high total serum IgE in a population from the Caribbean Coast of Colombia. Hum Genet (2009) 1.24
Heterogeneity in genetic admixture across different regions of Argentina. PLoS One (2012) 1.20
Attention-deficit/hyperactivity disorder and comorbid disruptive behavior disorders: evidence of pleiotropy and new susceptibility loci. Biol Psychiatry (2006) 1.12
Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas. Hum Mol Genet (2012) 1.11
Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease. Proc Natl Acad Sci U S A (2011) 1.08
Contrasting patterns of nuclear and mtDNA diversity in Native American populations. Ann Hum Genet (2010) 1.07
Cosmopolitan and ethnic-specific replication of genetic risk factors for asthma in 2 Latino populations. J Allergy Clin Immunol (2011) 1.03
Ushering in the study and treatment of preclinical Alzheimer disease. Nat Rev Neurol (2013) 1.03
Amerind ancestry, socioeconomic status and the genetics of type 2 diabetes in a Colombian population. PLoS One (2012) 1.02
Prevalence estimations of attention-deficit/hyperactivity disorder: differential diagnoses and comorbidities in a Colombian sample. Int J Neurosci (2003) 1.01
Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34. Hum Mol Genet (2006) 0.98
Phenotypic profile of early-onset familial Alzheimer's disease caused by presenilin-1 E280A mutation. J Alzheimers Dis (2012) 0.95
Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families. J Am Acad Child Adolesc Psychiatry (2004) 0.95
Comparison of the genetic background of different Colombian populations using the SNPforID 52plex identification panel. Int J Legal Med (2013) 0.95
Differential cerebral deposition of IDE and NEP in sporadic and familial Alzheimer's disease. Neurobiol Aging (2008) 0.95
CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. PLoS One (2013) 0.94
CA1 hippocampal neuronal loss in familial Alzheimer's disease presenilin-1 E280A mutation is related to epilepsy. Epilepsia (2004) 0.94
Neuropsychological study of familial Alzheimer's disease caused by mutation E280A in the presenilin 1 gene. Am J Alzheimers Dis Other Demen (2003) 0.94
Cortical atrophy in presymptomatic Alzheimer's disease presenilin 1 mutation carriers. J Neurol Neurosurg Psychiatry (2012) 0.93
Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate. Eur Child Adolesc Psychiatry (2007) 0.93
A revertant of the major founder Native American haplogroup C common in populations from northern South America. Am J Hum Biol (2006) 0.93
Deposition of hyperphosphorylated tau in cerebellum of PS1 E280A Alzheimer's disease. Brain Pathol (2011) 0.92
Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate. Hum Hered (2008) 0.92
Androgen receptor CAG and GGC polymorphisms in Mediterraneans: repeat dynamics and population relationships. J Hum Genet (2005) 0.90
Nongenetic factors as modifiers of the age of onset of familial Alzheimer's disease. Int Psychogeriatr (2003) 0.90
Specific deficit of colour-colour short-term memory binding in sporadic and familial Alzheimer's disease. Neuropsychologia (2011) 0.89
Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate. Psychiatr Genet (2010) 0.89
Population relationships in the Mediterranean revealed by autosomal genetic data (Alu and Alu/STR compound systems). Am J Phys Anthropol (2010) 0.89
Covert face recognition without the fusiform-temporal pathways. Neuroimage (2011) 0.88
[Validation of the Diagnostic Interview for Genetic Studies (DIGS) in Colombia]. Biomedica (2004) 0.88
Augmentation of bronchodilator responsiveness by leukotriene modifiers in Puerto Rican and Mexican children. Ann Allergy Asthma Immunol (2009) 0.88
Familial Alzheimer's disease-associated presenilin-1 alters cerebellar activity and calcium homeostasis. J Clin Invest (2014) 0.88
Linguistic changes in verbal expression: a preclinical marker of Alzheimer's disease. J Int Neuropsychol Soc (2007) 0.87
ERP generator anomalies in presymptomatic carriers of the Alzheimer's disease E280A PS-1 mutation. Hum Brain Mapp (2010) 0.87
Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations. Laryngoscope (2012) 0.86
Abundant mtDNA diversity and ancestral admixture in Colombian criollo cattle (Bos taurus). Genetics (2003) 0.86
Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate. Atten Defic Hyperact Disord (2011) 0.86
Putative association of the carboxy-terminal PDZ ligand of neuronal nitric oxide synthase gene (CAPON) with schizophrenia in a Colombian population. Schizophr Res (2005) 0.86
Dexamethasone inhibits apoptosis of human neutrophils induced by reactive oxygen species. Inflammation (2002) 0.85
Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls. Atten Defic Hyperact Disord (2012) 0.85
[Gene geography of Chile: regional distribution of American, European and African genetic contributions]. Rev Med Chil (2014) 0.84
Exploratory data from complete genomes of familial alzheimer disease age-at-onset outliers. Hum Mutat (2012) 0.84
Variations in the prevalence of metabolic syndrome in adolescents according to different criteria used for diagnosis: which definition should be chosen for this age group? Metab Syndr Relat Disord (2014) 0.83
Ultrastructure evidence of necrotic neural cell death in familial Alzheimer's disease brains bearing presenilin-1 E280A mutation. J Alzheimers Dis (2001) 0.83
Presenilin-1 280Glu-->Ala mutation alters C-terminal APP processing yielding longer abeta peptides: implications for Alzheimer's disease. Mol Med (2008) 0.82
Transmission distortion of BDNF variants to bipolar disorder type I patients from a South American population isolate. Am J Med Genet B Neuropsychiatr Genet (2006) 0.82
Cortical and subcortical diseases: do true neuropsychological differences exist? Arch Clin Neuropsychol (2005) 0.81
Alu insertions in the Iberian Peninsula and north west Africa--genetic boundaries or melting pot? Coll Antropol (2003) 0.81
Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate. Atten Defic Hyperact Disord (2009) 0.81
Cognitive changes in the preclinical phase of familial Alzheimer's disease. J Clin Exp Neuropsychol (2007) 0.81
ALOX5AP and LTA4H polymorphisms modify augmentation of bronchodilator responsiveness by leukotriene modifiers in Latinos. J Allergy Clin Immunol (2010) 0.81
The X chromosome Alu insertions as a tool for human population genetics: data from European and African human groups. Eur J Hum Genet (2007) 0.81
Extensive founder effect for distal renal tubular acidosis (dRTA) with sensorineural deafness in an isolated South American population. Am J Med Genet A (2008) 0.80
Autosomal recessive juvenile parkinsonism Cys212Tyr mutation in parkin renders lymphocytes susceptible to dopamine- and iron-mediated apoptosis. Mov Disord (2004) 0.80
Poorer cognitive performance in humans with mild cognitive impairment carrying the T variant of the Glu/Asp NOS3 polymorphism. Neurosci Lett (2004) 0.80
[Association between polymorphism in uncoupling proteins and type 2 diabetes in a northwestern Colombian population]. Biomedica (2009) 0.79
Brief communication: patterns of linkage disequilibrium and haplotype diversity at Xq13 in six Native American populations. Am J Phys Anthropol (2010) 0.79
A genetic cluster of early onset Parkinson's disease in a Colombian population. Am J Med Genet B Neuropsychiatr Genet (2006) 0.79
Lack of Association between Recurrent Pregnancy Loss and Inherited Thrombophilia in a Group of Colombian Patients. Thrombosis (2012) 0.78
Facial asymmetry and genetic ancestry in Latin American admixed populations. Am J Phys Anthropol (2015) 0.78
Analysis of Genomic Regions Associated With Coronary Artery Disease Reveals Continent-Specific Single Nucleotide Polymorphisms in North African Populations. J Epidemiol (2016) 0.78
Dual task abilities as a possible preclinical marker of Alzheimer's disease in carriers of the E280A presenilin-1 mutation. J Int Neuropsychol Soc (2011) 0.78
Genetic testing must recognize impact of bad news on recipient. Nature (2008) 0.78
Molecular variation at functional genes and the history of human populations--data on candidate genes for cardiovascular risk in the Mediterranean. Coll Antropol (2003) 0.78
Allele-allele interaction within the F13A1 gene: a risk factor for ischaemic heart disease in Spanish population. Thromb Res (2010) 0.77
The cognitive structure of time estimation impairments in adults with attention deficit hyperactivity disorder. Cogn Neuropsychol (2013) 0.77
The first homozygous family for prothrombin G20210A polymorphism reported in Latin America. Clin Appl Thromb Hemost (2008) 0.77
[Environmental risk factors and metabolic syndrome components in overweight youngsters]. Biomedica (2012) 0.77
The effect of genetic admixture in an association study: genetic polymorphisms and chromosome aberrations in a Colombian population exposed to organic solvents. Ann Hum Genet (2013) 0.76
Chromosome region 2p25 is linked and associated with type 1 diabetes in Colombia. J Genet (2010) 0.76
Segregation of a haplotype encompassing FEB1 with genetic epilepsy with febrile seizures plus in a Colombian family. Epileptic Disord (2013) 0.76
[Analysis of polymorphisms in the trypanothione reductase and cruzipain genes in Colombian strains of Trypanosoma cruzi]. Biomedica (2007) 0.76
Correction: Socioeconomic Status Is Not Related with Facial Fluctuating Asymmetry: Evidence from Latin-American Populations. PLoS One (2017) 0.75
[Biopercular syndrome caused by unilateral ischemia. Report of one case]. Rev Med Chil (2010) 0.75